Transfersome preparation for preventing and/or treating alopecia and preparation method and application thereof
A kind of technology of alopecia and transfer body, applied in the field of pharmaceutical preparations, can solve the problems of inability to act on the deep structure of hair follicles, limit the therapeutic effect of alopecia, and difficult to penetrate the cuticle of the skin, so as to achieve excellent anti-hair loss effect and promote the penetration of cutin layer, good stability
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Embodiment 1
[0068] Embodiment 1 Preparation of transfer body preparation (F1) of the present invention
[0069] The preparation method (film hydration method) is as follows:
[0070] (1) Add corticosterone-17α-propionate, Span80, and EPC to 12 mL of ethanol, and use a water-bath sonicator to sonicate for 5 minutes (ultrasonic power: 40 kHz) to ensure that all components are completely dissolved to obtain a mixture; in 12 mL of the mixture, The concentration of Span80 is 5% mg / mL, and the concentration of EPC is 95% mg / mL;
[0071] (2) Use a rotary evaporator (rotating speed 250rpm) to evaporate the ethanol under reduced pressure at 60° C., and obtain a continuous lipid film after the ethanol is completely evaporated;
[0072] (3) adding the lipid film to phosphate buffer (pH7.4) and ultrasonically treating it for 10 minutes to obtain a hydrated preparation, and then standing the hydrated preparation at room temperature for 30 minutes to obtain a primary medicinal solution;
[0073] (4) ...
Embodiment 2
[0075] Embodiment 2 Preparation of transfer body preparation (F2) of the present invention
[0076] Preparation method: refer to the preparation method of Example 1 to prepare the transfer body preparation of the present invention, referred to as F2, the difference is only that the lipid and edge activator types are replaced according to Table 1, and the corticosterone-17α-propane is controlled according to Table 1 Feed concentration of esters, lipids, edge activators.
Embodiment 3
[0077] Embodiment 3 Preparation of transfer body preparation (F3) of the present invention
[0078] Preparation method: refer to the preparation method of Example 1 to prepare the transfer body preparation of the present invention, referred to as F3, the only difference is that the lipid and edge activator types are replaced according to Table 1, and the corticosterone-17α-propane is controlled according to Table 1 Feed concentration of esters, lipids, edge activators.
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